Canonical Allele Identifier: CA2403929696

Gene: CACNG2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36564837T= , CM000684.2:g.36564837T=	GRCh38
NC_000022.10:g.36960884T= , CM000684.1:g.36960884T=	GRCh37
NC_000022.9:g.35290830T=	NCBI36
NG_031861.1:g.142807A=
NG_031861.2:g.143022A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300105.7:c.486A= MANE Select	ENSP00000300105.6:p.Gly162=
ENST00000300105.6:c.486A=	ENSP00000300105.6:p.Gly162=
NM_006078.3:c.486A=	NP_006069.1:p.Gly162=
NM_006078.4:c.486A=	NP_006069.1:p.Gly162=
XM_017028531.2:c.228A=	XP_016884020.1:p.Gly76=
NM_001379051.1:c.417A=	NP_001365980.1:p.Gly139=
NM_006078.5:c.486A= MANE Select	NP_006069.1:p.Gly162=
NR_166440.1:n.1852A=